A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv943893



Internal ID16237849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63830660..63836068hg38UCSC Ensembl
Innerchr20:62462013..62467421hg19UCSC Ensembl
Innerchr20:61932457..61937865hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385409
hg195409
hg185409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586651
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv943893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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